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- Klinische proef NCT07762014
rBCG-N-RSV Vaccine in Adults Aged 60 Years and Older
Randomized, Double-blind, Phase 2 Clinical Trial Controlled With Conventional Bacillus Calmette-Guérin (BCG) Vaccine to Evaluate the Safety and Immunogenicity of a Recombinant BCG Vaccine That Expresses the Respiratory Syncytial Virus (RSV) Nucleoprotein (N) (rBCG-N-RSV) in Adults Over 60 Years of Age.
Studie Overzicht
Toestand
Interventie / Behandeling
Studietype
Inschrijving (Geschat)
Fase
- Fase 2
Contacten en locaties
Studiecontact
- Naam: Maria Moukouli
- Telefoonnummer: +30 210 6560700
- E-mail: m.moukouli@pharmassist-cro.com
Studie Contact Back-up
- Naam: Maria Kiriakaki
- Telefoonnummer: +30 210 6560700
- E-mail: m.kiriakaki@pharmassist-cro.com
Studie Locaties
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Athens, Griekenland
- Werving
- Sotiria Thoracic Diseases Hospital of Athens
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Contact:
- Nikoletta Rovina, MD
- Telefoonnummer: +30 2107763100
- E-mail: nikrovina@med.uoa.gr
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Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
- Volwassen
- Oudere volwassene
Accepteert gezonde vrijwilligers
Beschrijving
Inclusion Criteria
- Has completed the written informed consent process.
- Males or females, over 60 years of age as of the date of signature of the informed consent form.
- Has a stable state of health or controlled (health parameters within the normal range for their disease) chronic diseases that do not fall within the exclusion criteria.
- Willingness to comply with study procedures.
- No plans to move to another city in the next 6 months and willing to be contacted by the research team within the study period.
- Not participate in another research study in the previous 3 months, nor plans to participate in another research study in the next 6 months.
- Agrees to avoid elective surgery during the study.
- Willingness to receive HIV test results.
- Not having received a BCG vaccination within the last 10 years before study vaccination.
Exlusion Criteria
- Oral temperature ≥37.5°C, axillary ≥37.5°C or tympanic temperature ≥38.0°C in the last 24 hours.
- Weight less than 50 kg, as well as BMI less than 18.5 or higher than 35 kg/m2.
- History of treatment or current history of active or latent tuberculosis infection.
- History of unprotected occupational exposure to an individual with active tuberculosis in a healthcare setting within the past 6 months.
- Immunosuppressive drugs used within the previous 42 days (inhaled and topical corticosteroids are allowed).
- Received documented investigational tuberculosis vaccine at any time.
- Unstable hormonal status, i.e. subjects with any change (dose, formulation, or route) in hormone replacement therapies (including levothyroxine, insulin, estrogen, progesterone etc.) in the last 12 weeks.
- History or laboratory evidence of any possible past, present, or future immunodeficiency status, including, but not limited to, any laboratory indication of HIV-1 infection.
- Allergy to BCG vaccine or its components, as well as the existence of contraindications for BCG administration as described in the BCG prescribing information.
- Previous medical history that may compromise the safety of the study participant, including but not limited to significant impairment of lung function (such as pulmonary diffusion of carbon dioxide <80% or FEV1 ≤80%) due to tuberculosis infection or other pulmonary disease; chronic heart disease with signs of heart failure (NYHA Class II Heart Failure or more) or coronary heart disease, suspicion of progressive neurological disease; uncontrolled epilepsy, liver disease.
- Administration of attenuated vaccines within 30 days before the start of the study or 14 days for inactivated ones.
- Having received transfusions or blood products within the 6 months before the start of the study.
- Uncontrolled hypertension or systolic blood pressure greater than 160 mmHg at the beginning of the study or diastolic greater than 90 mmHg.
- Active neoplasia.
- Stage 2 or higher chronic obstructive pulmonary disease.
- Chronic bronchial asthma with systemic corticosteroids, or with a history of having presented crises that have led to an emergency consultation within the last 2 months.
- Renal disease with estimated or relative creatinine clearance ≤ 70 ml/min x 1.73 m2.
- Evidence of a new acute illness that may compromise the safety of the study participant, such as fever (oral or axillary temperature greater than or equal to 37.5°C) or suspicion of active infection.
- History or laboratory evidence of chronic viral hepatitis.
- History of alcohol or drug abuse in the last 2 years.
- Smoking more than 30 cigarettes a day, or cannabis use three or more days a week.
- History of keloid formation.
- Congenital diseases of importance, such that they weaken the basal condition of the volunteer.
- Congenital or acquired absence of the spleen.
- Coagulation disorders or known thrombocytopenia of less than 100,000 platelets/mm3.
- Having undergone chemotherapy treatment in the last 6 months.
- Generalized urticaria in the last 2 months.
- History of hereditary or acquired angioneurotic edema.
- Any previous medical condition that the investigator considers may compromise the safety of the subject in the study.
- Not being available for all study visits (both face-to-face and by telephone) and specific instructions as appropriate (fasting, abstaining from intense physical exercise during the 24 hours before the study visits and during the 72 hours after vaccination).
- Pregnant women or women of childbearing potential (WOCBP) who are unable or unwilling to utilize appropriate methods of contraception during the study.
- Breast-feeding women.
- Male with heterosexual sexual activity with WOCBP who do not agree to use adequate contraception.
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Preventie
- Toewijzing: Gerandomiseerd
- Interventioneel model: Parallelle opdracht
- Masker: Verviervoudigen
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
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Experimenteel: rBCG-N-RSV vaccine
rBCG-N-RSV is a live-attenuated vaccine of Mycobacterium bovis bacillus Calmette-Guerin (BCG) modified to heterologously and constitutively express the RSV nucleoprotein (N). The clinical formulation with this bacterium has been produced under strict quality and safety standards using current Good Manufacturing Practices (cGMP) in the United States of America (USA). Pharmaceutical form: Lyophilisate for solution for injection Medicinal product characteristics: Immunological Route of administration: Intradermal use Maximum duration of treatment: 1 Day Maximum daily dose allowed: 0.1 Daily dose unit of measure: CFU/ml colony forming unit(s)/millilitre Maximum total dose allowed: 0.1 Total dose unit of measure: CFU/ml colony forming unit(s)/millilitre |
Intradermal vaccination with rBCG-N-RSV that expresses the N protein of the respiratory syncytial virus (RSV)
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Actieve vergelijker: Mycobacterium bovis bacillus Calmette-Guerin (BCG)
BCG is a cryo-lyophilized vaccine of an attenuated strain of Mycobacterium bovis BCG, used for active immunization against tuberculosis. It is currently administered in numerous countries worldwide according to national immunization plans. Medicinal product characteristics: Immunological Route of administration: Intradermal use Maximum duration of treatment: 1 Day Maximum daily dose allowed: 0.1 Daily dose unit of measure: CFU/ml colony forming unit(s)/millilitre Maximum total dose allowed: 0.1 Total dose unit of measure: CFU/ml colony forming unit(s)/millilitre |
Intradermal vaccination with conventional BCG (BCG-WT).
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Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Tijdsspanne |
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Occurrence, intensity, and duration of the local solicited AEs (evolution of the "flare-up") until the generation of the scar
Tijdsspanne: From vaccination through 180 days post-vaccination
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From vaccination through 180 days post-vaccination
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Occurrence, intensity and duration of unsolicited AEs during the 6-month follow-up.
Tijdsspanne: From vaccination through 180 days post-vaccination
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From vaccination through 180 days post-vaccination
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Occurrence of AEs during the 6-month follow-up duration.
Tijdsspanne: From vaccination through 180 days post-vaccination
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From vaccination through 180 days post-vaccination
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Alterations to the hemogram and/or biochemical profile at 30- and 180- days post vaccination compared to pre-vaccination profile
Tijdsspanne: Day 30 and day 180 post-vaccination
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Day 30 and day 180 post-vaccination
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Production of IFN-γ and IL-2 by T cells upon exposure to purified protein derivative (PPD) mycobacterial antigen via ELISPOT 7 days prior vaccination and 30- and 180-days post vaccination.
Tijdsspanne: Day 30 and day 180 post-vaccination
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Day 30 and day 180 post-vaccination
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Production of IFN-γ and IL-2 by T cells upon exposure to recombinant RSV nucleoprotein antigen via ELISPOT 7 days prior vaccination and 30- and 180-days post vaccination
Tijdsspanne: Day 30 and day 180 post-vaccination
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Day 30 and day 180 post-vaccination
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Secundaire uitkomstmaten
Uitkomstmaat |
Tijdsspanne |
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Presence and titers of serum IgG antibodies against Purified Protein Derived Mycobacterial antigen (PPD) via ELISA
Tijdsspanne: Day 30 and day 180 post-vaccination
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Day 30 and day 180 post-vaccination
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Presence and titers of serum IgG against RSV nucleoprotein via ELISA.
Tijdsspanne: Day 30 and day 180 post-vaccination
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Day 30 and day 180 post-vaccination
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Andere uitkomstmaten
Uitkomstmaat |
Tijdsspanne |
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Cases of symptomatic RSV infection confirmed by RT-qPCR detection in respiratory specimens from 14 days to 6 months after vaccination.
Tijdsspanne: From day 14 to 6 months post-vaccination
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From day 14 to 6 months post-vaccination
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Cases of hospitalization/intensive care unit admission and/or death in participants with RSV infection confirmed by RT-qPCR in vaccinated subjects from 14 days to 6 months postvaccination
Tijdsspanne: From day 14 to 6 months post-vaccination
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From day 14 to 6 months post-vaccination
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Increase in the percentage of specific CD4+ and CD8+ T cells that express AIM and memory markers via flow cytometry in the peripheral blood of a subgroup of participants that receive the control and the study vaccine.
Tijdsspanne: Day 30 and day 180 post-vaccination
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Day 30 and day 180 post-vaccination
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Medewerkers en onderzoekers
Studie record data
Bestudeer belangrijke data
Studie start (Werkelijk)
Primaire voltooiing (Geschat)
Studie voltooiing (Geschat)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Werkelijk)
Updates van studierecords
Laatste update geplaatst (Werkelijk)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Aanvullende relevante MeSH-voorwaarden
- Infecties
- Gram-positieve bacteriële infecties
- Bacteriële infecties
- Bacteriële infecties en mycosen
- Actinomycetales-infecties
- Mycobacterium-infecties
- Tuberculose
- Onderzoekstechnieken
- Therapeutica
- Volksgezondheid
- Milieu en volksgezondheid
- Gezondheidsdiensten
- Gezondheidszorgfaciliteiten personeel en diensten
- Preventieve gezondheidsdiensten
- Biologische therapie
- Immunologische technieken
- Public Health Practice
- Immunomodulatie
- Primaire preventie
- Immunisatie
- Immunotherapie
- Immunotherapie, actief
- Controle van overdraagbare ziekten
- Vaccinatie
Andere studie-ID-nummers
- rBCG-N-RSV 002GR
- 2023 (Subsidie/contract van de Amerikaanse NIH: GRAMMY Museum Foundation)
- 2023-509048-80-01 (Ctis)
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
Beschrijving IPD-plan
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
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